NDC 73581-027 – Fexofenadine Hydrochloride

Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC73581-027

Product details

Brand name
Fexofenadine Hydrochloride
Generic name
Fexofenadine Hydrochloride
Labeler
YYBA Corp
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210137
Marketed since
October 1, 2024
Listing expires
December 31, 2027
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Fexofenadine Hydrochloride →

Package NDC codes (4)

Package NDCDescriptionSince
73581-027-0110 TABLET in 1 BOTTLE (73581-027-01)Oct 3, 2025
73581-027-0440 TABLET in 1 BOTTLE (73581-027-04)Oct 3, 2024
73581-027-10100 TABLET in 1 BOTTLE (73581-027-10)Oct 3, 2025
73581-027-20200 TABLET in 1 BOTTLE (73581-027-20)Oct 29, 2025

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